Top 67 Clinical trial manager Jobs in Morrisville Nc

Clinical Trial Manager - CAR T or Ophthalmology
Fortrea —Durham, NC
- $76,000 - $148,000 a year
- Full-time
- Remote
- English
- 3 years
- Master's degree
Clinical Trial Manager
InfoQuest Consulting Group Inc. —Durham, NC
- Email
- Contracts
- Senior level
Manager, Clinical Operations
IQVIA —Durham, NC
- $86,500 - $216,000 a year
- Full-time
- Remote
- Microsoft Excel
- English
- Mid-level
- Work from home
Clinical Trials Manager
Kite Pharma —Raleigh, NC
- $133,195 - $189,640 a year
- Full-time
- 6 years
- Surgery
- RN License
- Health insurance
- Dental insurance
RWE Clinical Project Manager – Oncology (FSP)
IQVIA —Durham, NC
- $93,100 - $232,800 a year
- Full-time
- Remote
- Mid-level
- Bachelor's degree
- Continuous improvement
- Work from home
Senior Clinical Data Manager
Fortrea —Durham, NC
- $85,000 - $120,000 a year
- Full-time
- Remote
- Customer service
- English
- Bachelor's degree
- Disability insurance
- Health insurance
10d
Clinical Project Manager (US)
Alimentiv —Raleigh-Durham, NC
- $95,500 - $159,000 a year
- Full-time
- Remote
- English
- Mid-level
- Bachelor's degree
Quick Apply
Clinical Project Manager- IVD
IQVIA —Durham, NC
- $93,100 - $232,800 a year
- Full-time
- Remote
- Bachelor's degree
- 1 year
- Senior level
- Work from home
Clinical Project Manager, Immuno-Oncology - IQVIA Biotech
IQVIA —Durham, NC
- $93,100 - $232,800 a year
- Full-time
- Remote
- Customer service
- Bachelor's degree
- Continuous improvement
- Work from home
Clinical Project Manager
Pluto Health —Durham, NC
- $85,000 - $120,000 a year
- Full-time
- 3 years
- Analysis skills
- Senior level
- Paid holidays
- Health insurance
Associate Manager / Manager, Project Services - Laboratories (Remote - East Coast)
IQVIA —Durham, NC
- $64,200 - $173,000 a year
- Full-time
- Remote
- Microsoft Excel
- Computer literacy
- Data analysis skills
- Work from home
Senior Clinical Project Manager
IQVIA —Durham, NC
- $93,100 - $232,800 a year
- Full-time
- Remote
- Bachelor's degree
- Mentoring
- Senior level
- Work from home
11d
Senior Clinical Project Manager, Immuno-Oncology, IQVIA Biotech
IQVIA —Durham, NC
- $93,100 - $232,800 a year
- Full-time
- Remote
- 7 years
- Microsoft Office
- Bachelor's degree
- Work from home
Senior Global Clinical Study Manager
IQVIA —Durham, NC
- $93,100 - $232,800 a year
- Full-time
- Remote
- Bachelor's degree
- Continuous improvement
- Mentoring
- Work from home
Project Manager I, RWE
サイネオス・ヘルス —Morrisville, NC
- Nursing
- Medicine
- English
(Senior) Clinical Study Manager, Clinical Development
Tempus —Research Triangle Park, NC
- $110,000 - $160,000 a year
- Full-time
- Nursing
- 5 years
- HIPAA
- Health insurance
4d
Site Activation Manager
IQVIA —Durham, NC
- $86,500 - $216,000 a year
- Full-time
- Remote
- Bachelor's degree
- Team management
- Mentoring
- Work from home
Clinical Lead- CVRM
IQVIA —Durham, NC
- $93,100 - $232,800 a year
- Full-time
- Remote
- Microsoft Excel
- 5 years
- English
- Work from home
Senior Clinical Data Manager
Worldwide Clinical Trials —Research Triangle Park, NC
- $79,000 - $157,000 a year
- Full-time
- Computer science
- Computer Science
- 5 years
Senior Clinical Project Manager- CNS
IQVIA —Durham, NC
- $93,100 - $232,800 a year
- Full-time
- Remote
- Microsoft Excel
- English
- Bachelor's degree
- Work from home

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Clinical Trial Manager - CAR T or Ophthalmology

Fortrea -
Durham, NC

Apply Now

Job Details

Full-time
$76,000 - $148,000 a year

Qualifications

Research project team leadership
English
Global team management
ICH guidelines
Project management experience in healthcare
Client management
Managing clinical research teams
Leading team collaboration initiatives
Productivity software
Clinical quality assurance standards
International corporation experience
Pharmaceutical research experience
Team motivation (leadership skill)

Full Job Description

Fortrea is seeking Clinical Trial Managers to join our team! We are seeking experienced CTLs with 3+ years of experience. . Remote US or Canadian based. We are seeking candidates with either CAR T or Ophthalmology experience.

Job Overview:

The Clinical Trial Manager has ownership in the clinical delivery and operational oversight of clinical research trials. This role collaborates with project managers and other functional leads to deliver clinical and start-up activities within budget and contract, ensuring quality, compliance and meeting country-specific commitments.

The role generally works under the direction of a (Senior) Clinical Trial Manager, however, may also work independently at a lower complexity study.

Summary of Responsibilities:

End-to-end oversight of start-up and clinical responsibilities—from site identification through to database lock—through proactive management of project scope, timelines, milestones, and budget.
Ensure start-up and clinical project plans address identified risks while adhering to professional standards, SOPs, client, and regulatory requirements.
Proactively identify and address start-up and clinical project, financial, and quality risks by applying comprehensive risk management strategies and ensuring compliance, including tracking within applicable systems.
Responsible for financial aspects of clinical and start-up activities, including revenue forecasting, adherence to contracted scope, and oversight of scope modifications.
Ensure project team awareness and tracking of Key Project Indicators (KPI) for any client-specific start-up and clinical metrics.
Ensure and plans for start-up and clinical resources with accurate projections for the resourcing teams.
Develop and implement the site activation and recruitment strategy in collaboration with project teams.
Lead and oversee site identification and site selection.
Oversight of Informed Consent Form development and translations.
Oversight of essential document creation and collection, including insurance.
Oversight of the development, negotiation, and execution of Clinical Trial Agreements (CTA), including site budgets.
Lead the end-to-end process of regulatory/ethics committee submissions, approvals, and tracking.
Ensure clinical and ancillary supplies -including import/export logistics and supply destruction processes- are in place as applicable.
Manage operational aspects to support subject recruitment and retention, patient safety, vendor performance, and the monitoring visit strategy.
Proactive planning for monitoring activities to ensure data integrity, patient safety and endpoint protection.
Ensure inspection-readiness through quality oversight of TMF, monitoring reports, protocol deviations and issue management.
Oversight and approval of site payments, including payment reconciliation.
Foster effective communication and collaboration with clients and cross-functional project teams in a global and multicultural environment.
Ability to lead client-facing calls to communicate project status updates and demonstrate operational control of start-up and clinical deliverables.
Support new business with active participation in pre-award preparation as required.
Provide feedback on team members as needed to respective line managers.
All other duties as needed or assigned.

Qualifications (Minimum Required):

University/college degree (life science preferred) or certification in a related allied health profession (nursing, medical, or laboratory technology) from an appropriately accredited institution.
Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
Fluent in English, both written and verbal

Experience (Minimum Required):

Four or more years of relevant clinical research experience in pharmaceutical, CRO, or health care setting will be considered.
Previous SSU and Clinical Trial Lead experience
CAR T or Ophthalmology experience
Comprehensive knowledge of GCP, ICH, and regulatory guidelines.
Proficiency in Microsoft Office and familiarity with EDC, CTMS, eTMF, and vendor platforms (e.g. Veeva Vault, Medidata).
Effective leadership in remote and global environment.
Strong communication, planning, and organizational abilities.
Proven team motivational skills.
Proficiency in balancing concurrent tasks within time-sensitive environments.
Financial awareness and use of tracking systems/tools.
Demonstrated independent problem-solving and risk management mindset.
Demonstrated professional client interaction and presentation skills, with ability to work independently and collaboratively.

In this role, employees will leverage their existing experience and skills to assume additional responsibilities within the broader role. These will be aligned with operational requirements and internal training, without altering the fundamental nature or classification of the position.

Preferred Qualifications Include:

Master’s or other advanced degree.
PMP certification or equivalent.

Physical Demands / Work Environment:

Remote-based work required with possible office presence depending on location.
Travel requirements: up to 20% (global – primarily domestic and international)

Pay Range: $76,000 - 148,000 USD annually

Learn more about our EEO & Accommodations request here .

Apply Now

Refine Your Search

clinical trial manager jobs in morrisville nc

Clinical Trial Manager - CAR T or Ophthalmology

Clinical Trial Manager

Manager, Clinical Operations

Clinical Trials Manager

RWE Clinical Project Manager – Oncology (FSP)

Senior Clinical Data Manager

Clinical Project Manager (US)

Clinical Project Manager- IVD

Clinical Project Manager, Immuno-Oncology - IQVIA Biotech

Clinical Project Manager

Associate Manager / Manager, Project Services - Laboratories (Remote - East Coast)

Senior Clinical Project Manager

Senior Clinical Project Manager, Immuno-Oncology, IQVIA Biotech

Senior Global Clinical Study Manager

Project Manager I, RWE

(Senior) Clinical Study Manager, Clinical Development

Site Activation Manager

Clinical Lead- CVRM

Senior Clinical Data Manager

Senior Clinical Project Manager- CNS

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Fortrea is seeking Clinical Trial Managers to join our team! We are seeking experienced CTLs with 3+ years of experience. . Remote US or Canadian based. We are seeking candidates with either CAR T or Ophthalmology experience.

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